携带免疫球蛋白和补体受体的淋巴细胞在人类外周血中构成同一群体。
Immunoglobulin-bearing and complement-receptor lymphocytes constitute the same population in human peripheral blood.
作者信息
Ehlenberger A G, McWilliams M, Phillips-Quagliata J M, Lamm M E, Nussenzweig V
出版信息
J Clin Invest. 1976 Jan;57(1):53-6. doi: 10.1172/JCI108268.
Abstract
Complement-receptor lymphocytes have generally been considered to be a subpopulation of bone-marrow derived (B) lymphocytes. However, the present studies show that essentially all cells with integral surface immunoglobulin from normal human peripheral blood bear receptors for the third component of complement. Moreover, after removal of phagocytes, all cells with complement receptors bear surface Ig. Thus, circulating B cells and complement-receptor lymphocytes are the same population.
摘要
补体受体淋巴细胞通常被认为是骨髓来源的（B）淋巴细胞亚群。然而，目前的研究表明，来自正常人外周血的所有带有完整表面免疫球蛋白的细胞实际上都带有补体第三成分的受体。此外，去除吞噬细胞后，所有带有补体受体的细胞都带有表面免疫球蛋白。因此，循环B细胞和补体受体淋巴细胞是同一群体。
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Immunoglobulin-bearing and complement-receptor lymphocytes constitute the same population in human peripheral blood.携带免疫球蛋白和补体受体的淋巴细胞在人类外周血中构成同一群体。
J Clin Invest. 1976 Jan;57(1):53-6. doi: 10.1172/JCI108268.
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Binding of sheep red blood cells to a large population of human lymphocytes.绵羊红细胞与大量人类淋巴细胞的结合。
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Receptors for immune complexes on lymphocytes.淋巴细胞上免疫复合物的受体
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Immunoglobulin D as a lymphocyte receptor.作为淋巴细胞受体的免疫球蛋白D
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Localization of free and bound secretory component in human intestinal epithelial cells. A model for the assembly of secretory IgA.人肠上皮细胞中游离及结合分泌成分的定位。分泌型IgA组装的一种模型。
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Membrane immunoglobulins and antigen receptors on B and T lymphocytes.B淋巴细胞和T淋巴细胞上的膜免疫球蛋白及抗原受体。
Adv Immunol. 1974;19(0):67-216. doi: 10.1016/s0065-2776(08)60252-7.
9
Interaction of aggregated -globulin with B lymphocytes.聚集的γ球蛋白与B淋巴细胞的相互作用。
J Exp Med. 1972 Jul 1;136(1):191-6. doi: 10.1084/jem.136.1.191.
10
Cell surface immunoglobulin. XI. The appearance of an IgD-like molecule on murine lymphoid cells during ontogeny.细胞表面免疫球蛋白。XI. 小鼠淋巴样细胞个体发育过程中类IgD分子的出现。
J Exp Med. 1975 Jan 1;141(1):206-15. doi: 10.1084/jem.141.1.206.
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